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FDA 510(k), K833430, BLOOD GAS EXPERSYSTEM 8700
FDA 510(k), K833430, BLOOD GAS EXPERSYSTEM 8700
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510(K) Number: K833430
Device Name: BLOOD GAS EXPERSYSTEM 8700
Manufacturer: MEDICAL INTELCOM, INC.
Device Classification Name: stimulator, spinal-cord, implanted for peripheral vascular disease
Regulation Number:
Classification Product Code: LLE
Date Received: 10/05/1983
Decision Date: 02/10/1984
Regulation Medical Specialty:
Device Name: BLOOD GAS EXPERSYSTEM 8700
Manufacturer: MEDICAL INTELCOM, INC.
Device Classification Name: stimulator, spinal-cord, implanted for peripheral vascular disease
Regulation Number:
Classification Product Code: LLE
Date Received: 10/05/1983
Decision Date: 02/10/1984
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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